Buspirone Hydrochloride

Product NDC
50090-7161
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Buspirone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA210907
Marketing category
ANDA
Substance
BUSPIRONE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7161-160 TABLET in 1 BOTTLE (50090-7161-1) 2024-05-06NoHistorical
50090-7161-390 TABLET in 1 BOTTLE (50090-7161-3) 2024-05-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Buspirone Hydrochloride Tablets, USP Rx OnlyA-S Medication Solutions2024-05-06HUMAN PRESCRIPTION DRUG LABEL6